食品科学 ›› 2011, Vol. 32 ›› Issue (11): 198-203.doi: 10.7506/spkx1002-6630-201111042

• 生物工程 • 上一篇    下一篇

乳源性免疫活性肽在E.coli BL21中分泌表达的诱导条件优化

胡 迪,张少辉*   

  1. 上海交通大学农业与生物学院
  • 出版日期:2011-06-15 发布日期:2011-05-13
  • 基金资助:
    国家“863”计划项目(008AA10Z329)

Optimization of Expression Conditions for Milk-derived Immune Peptides in E. coli BL21

HU Di,ZHANG Shao-hui*   

  1. School of Agriculture and Biology, Shanghai JiaoTong University, Shanghai 200240, China
  • Online:2011-06-15 Published:2011-05-13

摘要: 设计4个乳源性免疫活性肽的目的基因后,利用基因重组技术成功构建原核表达载体pTYB11,并将重组质粒转化到E.coli BL21中,通过改变异丙基-β-D-硫代吡喃半乳糖苷 (IPTG)的浓度、培养时间和培养温度,设计正交试验来优化乳源活性小肽的IPTG诱导表达条件,使目的蛋白可在E.coli BL21中高效表达。依据15% SDS-PAGE电泳分析得到融合蛋白的表达量,选出最适诱导条件为IPTG终浓度0.1~0.2mmol/L,在12~15℃条件下培养20h,得到大小为59.2kD左右的融合目的蛋白,其表达量可占总蛋白表达量的40%,经Western Blotting鉴定正确。

关键词: 乳源性免疫活性肽, pTYB11, 原核表达, IPTG, 诱导条件优化

Abstract: The target genes of 4 previously reported milk-derived immuno-modulating peptides were designed, and the prokaryotic expression plasmid pTYB11 with the target genes was then constructed and transformed into E. coli BL21 by recombinant DNA technique. Expression conditions such as IPTG concentration, expression temperature and expression time of the plasmid encoded milk-derived immune peptides in E. coli BL21 cells were optimized by orthogonal array design. The quantitative analysis of the fusion protein by 15% SDA-PAGE showed that the optimal expression conditions were the induction of IPTG at the concentration of 0.1-0.2 mmol/L, and expression temperature of 12-15℃ for 20 h. A 59.2 kD fusion protein was identified in Western Blotting and its expression amount was found to account for 40% of total proteins.

Key words: milk-derived immune peptide, pTYB11, prokaryotic expression, IPTG, optimization of induction conditions

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